A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202914



Internal ID21341717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163230732..163230732hg38UCSC Ensembl
chr6:163651764..163651764hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931352
Supporting Variants
SamplesHG002
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202914
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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